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Cathepsin B, Human Liver

Cathepsin B, Human Liver, CAS 9047-22-7, is a purified native cathepsin B from human liver, purified by affinity chromatography. Upregulated in many types of tumors.

Synonim(y):

Cathepsin B, Human Liver, cat B, cysteine cathepsin

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Gabaryty przesyłkiSKUDostępnośćCena netto
50 μg

Dostępne do wysyłki DZISIAJzKuehne + Nagel Sp. z o.o.

2110,00 zł

Informacje o tej pozycji

Numer CAS:
NACRES:
NA.77
UNSPSC Code:
12352202
MDL number:
Specific activity:
≥10 units/mg protein
Assay:
≥95% (SDS-PAGE)
Biological source:
human liver

2110,00 zł


Dostępne do wysyłki DZISIAJSzczegóły


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biological source

human liver

Quality Level

description

Merck USA index - 14, 1905

assay

≥95% (SDS-PAGE)

form

liquid

specific activity

≥10 units/mg protein

purified by

affinity chromatography

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, avoid repeated freeze/thaw cycles

technique(s)

activity assay: suitable

suitability

suitable for molecular biology

application(s)

life science and biopharma

shipped in

wet ice

storage temp.

−70°C

Gene Information

human ... CTSB(1508)

General description

Research area: Cell Signaling

Native cathepsin B from human liver, purified by affinity chromatography and HPLC. The most investigated enzyme of all lysosomal cysteine proteases. Cathepsin B belongs to the papain-like family of cysteine proteases and is produced as a preproenzyme. It is a bilobal protein, and its catalytic site is situated at the interface between the two lobes.

Application

Cathepsin B, Human Liver, has been used in:
  • Diagnostics: as a potent and independent prognostic marker for endometrial cancer, pancreatic adenocarcinoma, and inflammatory disease.
  • Drug development: during the neovascularization process and as a potent therapeutic target for various pathologies, cancer progression, and osteoarthritis in humans.
  • Pharmacology: for increasing the therapeutic index of doxorubicin by incorporating the cathepsin B cleavable spacer Phe-Lys-4-aminobenzyloxycarbonyl into an albumin-binding prodrug.
  • Molecular biology: in cathepsin B activity assay.

Biochem/physiol Actions

Cathepsin B acts as both endo and exopeptidase. While as an endopeptidase it cleaves amino acids with a large hydrophobic side chain in the P2 site of the protein/peptide substrate, on the other hand as an exopeptidase it eliminates two amino acids (dipeptide) from the C terminus of a polypeptide substrate, thereby categorizing the enzyme as a peptidyl dipeptidase. It maintains homeostatic metabolic activity within cells through regular turnover of both intracellular and extracellular proteins. Additionally, it is involved in various cellular functions like regulation of pro-enzyme and pro-hormone activation, tissue remodeling, antigen processing, apoptosis, and inflammatory responses to antigens. The expression and activity of cathepsin B have been linked to several pathologies, including cardiovascular disease, cancer, Alzheimer’s, arthritis, and pancreatitis. Overexpression of cathepsin B has been observed in brain, breast, gastric, prostate, esophageal, skin, lung, ovarian, colon, and thyroid cancers and correlates positively with their invasive and metastatic capabilities. Cathepsin B is shown to facilitate tumor invasion by dissolving extracellular barriers.

Physical form

In 50 mM sodium acetate buffer, 1 mM EDTA, pH 5.0.

Preparation Note

Following initial thaw, aliquot and freeze (-70°C).
Prepared from tissues of individuals that have been shown by certified tests to be negative for HBsAg and for antibodies to HIV and HCV.

Other Notes

Hirai, K., et al. 1999. Hum. Pathol.30, 680.
Kostoulas, G., et al. 1999. FEBS Lett.455, 286.
Strojnik, T., et al. 1999. Clin. Cancer Res.5, 559.
Maquire, T.M., et al. 1998. Int. J. Biol. Markers13, 139.
Berquim, I.M., and Sloane, B.F. 1996. Adv. Exp. Med. Biol.389, 281.
One unit is defined as the amount of enzyme that will hydrolyze 1.0 µmol Z-RR-β-naphthylamide per min at 40°C, using 100 mM Na+/K+ pH 6.0, with 1.33 mM EDTA and 2 mM DTT as the activation buffer.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)
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Ta pozycja
C8571SRP0289C0150
specific activity

≥10 units/mg protein

specific activity

≥200 units/mg protein (One unit is defined as the amount of enzyme that hydrolyzes 1 μmol of Z-Arg-Arg-beta-naphthylamide per minute at 40 °C, using 100 mM Na/K phosphate, pH 6.0, with 1.33 mM EDTA and 2 mM DTT as the activation buffer.)

specific activity

≥2228 pmol/min-μg

specific activity

≥5 units/mg protein

biological source

human liver

biological source

human liver

biological source

human

biological source

-

assay

≥95% (SDS-PAGE)

assay

-

assay

≥90% (SDS-PAGE)

assay

-

Gene Information

human ... CTSB(1508)

Gene Information

human ... CTSB(1508)

Gene Information

human ... CTSB(1508)

Gene Information

human ... CTSB(1508)

technique(s)

activity assay: suitable

technique(s)

-

technique(s)

activity assay: suitable

technique(s)

-

suitability

suitable for molecular biology

suitability

-

suitability

suitable for molecular biology

suitability

-


Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Odwiedź Bibliotekę dokumentów



Cathepsin B: Basis Sequence: Mouse
Cavallo-Medved D, et al.
The AFCS-nature Molecule Pages (2011)
Zsanett Jancsó et al.
Gastroenterology, 158(4), 1083-1094 (2019-11-22)
Mutations in the human serine protease 1 gene (PRSS1), which encodes cationic trypsinogen, can accelerate its autoactivation and cause hereditary or sporadic chronic pancreatitis. Disruption of the locus that encodes cationic trypsinogen in mice (T7) causes loss of expression of



Numer pozycji handlu globalnego

SKUNUMER GTIN
219362-50UG04055977202205

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